Advertisements
Advertisements
प्रश्न
Match the reactions given in Column I with the suitable reagents given in Column II.
| Column I (Reactions) |
Column II (Reagents) |
| (i) Benzophenone Diphenylmethane | (a) \[\ce{LiAlH4}\] |
| (ii) Benzaldehyde 1-Phenylethanol | (b) \[\ce{DIBAL-H}\] |
| (iii) Cyclohexanone Cyclohexanol | (c) \[\ce{Zn(Hg)/Conc. HCl}\] |
| (iv) Phenyl benzoate Benzaldehyde | (d) \[\ce{CH3MgBr}\] |
Advertisements
उत्तर
| Column I (Reactions) |
Column II (Reagents) |
| (i) Benzophenone Diphenylmethane | (c) \[\ce{Zn(Hg)/Conc. HCl}\] |
| (ii) Benzaldehyde 1-Phenylethanol | (d) \[\ce{CH3MgBr}\] |
| (iii) Cyclohexanone Cyclohexanol | (a) \[\ce{LiAlH4}\] |
| (iv) Phenyl benzoate Benzaldehyde | (b) \[\ce{DIBAL-H}\] |
Explanation:
(i)
(ii)
(iii)
(iv)
APPEARS IN
संबंधित प्रश्न
Write the structures of A and B in the following reactions
Name the reagents used in the following reactions:
Show how the following compound can be converted to benzoic acid.
Acetophenone
Show how the following compound can be converted to benzoic acid.
Bromobenzene
Predict the products formed when cyclohexanecarbaldehyde reacts with the following reagent.
Tollens’ reagent
How will you prepare the given compound from benzene? You may use any inorganic reagent and any organic reagent having not more than one carbon atom.
Methyl benzoate
How will you prepare the given compound from benzene? You may use any inorganic reagent and any organic reagent having not more than one carbon atom.
p-Nitrobenzoic acid
How will you bring about the following conversion in not more than two steps?
Benazaldehyde to α-Hydroxyphenylacetic acid
What is the action of following reagents on glucose?
1. Bromine water
2. Hydroxylamine
The reagent which does not react with both, acetone and benzaldehyde.
Through which of the following reactions number of carbon atoms can be increased in the chain?
(i) Grignard reaction
(ii) Cannizaro’s reaction
(iii) Aldol condensation
(iv) HVZ reaction
Assertion: Aldehydes and ketones, both react with Tollen’s reagent to form silver mirror.
Reason: Both, aldehydes and ketones contain a carbonyl group.
Which of the following substance produced acetaldehyde on dry distillation?
Match List - I with List - II.
| List - I | List - II | ||
| (a) |  \[\ce{->[CO,HCl][Anhyd. AlCl3/CuCl]}\] |
(i) | Hell-Volhard-Zelinsky reaction |
| (b) |
\[\begin{array}{cc}
\ce{O}\phantom{.................}\\ ||\phantom{.................}\\ \ce{R - C - CH3 + NaOX ->} \end{array}\] |
(ii) | Gattermann-Koch reaction |
| (c) | \[\ce{R - CH2 - OH + R'COOH ->[Conc. H2SO4]}\] | (iii) | Haloform reaction |
| (d) | \[\ce{R - CH2COOH ->[(i) X2/Red P][(ii) H2O]}\] | (iv) | Esterification |
Choose the correct answer from the options given below.
The end product Y in the sequence of reaction:
\[\ce{RX ->[CN^-] X ->[NaOH] Y}\] is:
Y is:
Hex-4-ene-2-ol on treatment with PCC gives 'A'. 'A' on reaction with sodium hypoiodite gives 'B', which on further heating with soda lime gives 'C. The compound 'C' is ______.
Fill in the blanks by choosing the appropriate words from those given in the brackets:
[stable, low, aldehyde, unstable, 6, 4, ethane, Clemmensen’s, 2, 3, carboxylic acid, high, propane, Rosenmund's]
The primary alcohols are easily oxidised first into ______ and then into ______.
